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lurasidone hydrochloride

NDC 68180-671 · Lupin Pharmaceuticals, Inc.

Generic namelurasidone hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)LURASIDONE HYDROCHLORIDE
Strength40 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

68180-671-06 — 30 TABLET in 1 BOTTLE (68180-671-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-957 — LURASIDONE HYDROCHLORIDE, 67046-1637 — Lurasidone Hydrochloride, 67046-1654 — LURASIDONE HYDROCHLORIDE, 67046-1659 — Lurasidone Hydrochloride, 67877-638 — lurasidone hydrochloride, 67877-639 — lurasidone hydrochloride, 67877-640 — lurasidone hydrochloride, 67877-641 — lurasidone hydrochloride, 67877-642 — lurasidone hydrochloride, 68180-670 — lurasidone hydrochloride, 68180-672 — lurasidone hydrochloride, 68180-673 — lurasidone hydrochloride, 68180-674 — lurasidone hydrochloride, 68382-859 — Lurasidone hydrochloride, 68382-965 — Lurasidone hydrochloride, 68382-966 — Lurasidone hydrochloride, 68382-967 — Lurasidone hydrochloride, 68382-968 — Lurasidone hydrochloride, 69097-937 — Lurasidone Hydrochloride, 69097-938 — Lurasidone Hydrochloride, +117 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.